solu-cortef

Generic: hydrocortisone sodium succinate

Labeler: pharmacia & upjohn company llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name solu-cortef
Generic Name hydrocortisone sodium succinate
Labeler pharmacia & upjohn company llc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

hydrocortisone sodium succinate 500 mg/4mL

Manufacturer
Pharmacia & Upjohn Company LLC

Identifiers & Regulatory

Product NDC 0009-0016
Product ID 0009-0016_8512044a-4a54-4634-bb97-9e20126adc61
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA009866
Listing Expiration 2026-12-31
Marketing Start 1955-04-27

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00090016
Hyphenated Format 0009-0016

Supplemental Identifiers

RxCUI
105398 238755 1738586 1738589 1738590 1738592 1738594 1738596
UPC
0300090016128 0300090013059 0300090005016
UNII
50LQB69S1Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name solu-cortef (source: ndc)
Generic Name hydrocortisone sodium succinate (source: ndc)
Application Number NDA009866 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/4mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (0009-0016-12) / 4 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

0009-0016-12 1 VIAL, SINGLE-DOSE in 1 CARTON (0009-0016-12) / 4 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

hydrocortisone sodium succinate (500 mg/4mL)

Linked Drug Pages (1)

Solu-Cortef ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "8512044a-4a54-4634-bb97-9e20126adc61", "openfda": {"upc": ["0300090016128", "0300090013059", "0300090005016"], "unii": ["50LQB69S1Z"], "rxcui": ["105398", "238755", "1738586", "1738589", "1738590", "1738592", "1738594", "1738596"], "spl_set_id": ["65eefd58-b166-4d71-ade6-45c8fdf86922"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0009-0016-12)  / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0009-0016-12", "marketing_start_date": "19550427"}], "brand_name": "Solu-Cortef", "product_id": "0009-0016_8512044a-4a54-4634-bb97-9e20126adc61", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0009-0016", "generic_name": "hydrocortisone sodium succinate", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Solu-Cortef", "active_ingredients": [{"name": "HYDROCORTISONE SODIUM SUCCINATE", "strength": "500 mg/4mL"}], "application_number": "NDA009866", "marketing_category": "NDA", "marketing_start_date": "19550427", "listing_expiration_date": "20261231"}